BBa_K2044002BBa_K2044002 Version 1 (Component)Based on our project, <2,1> is the direct pathway from Site No.2 to Site No.1 in the map we design.
BBa_K2044005BBa_K2044005 Version 1 (Component)Based on our project, <2,6> is the direct pathway from Site No.2 to Site No.6 in the map we design.
BBa_K2044012BBa_K2044012 Version 1 (Component)Based on our project, <6,8> is the direct pathway from Site No.6 to Site No.8 in the map we design.
BBa_K2044011BBa_K2044011 Version 1 (Component)Based on our project,<6,4> is the direct pathway from Site No.6 to Site No.4 in the map we design.
BBa_K1172306BBa_K1172306 Version 1 (Component)Riboflavin synthesis gene cluster from s. oneidensis under control of a strong Anderson promoter
BBa_K1172305BBa_K1172305 Version 1 (Component)Riboflavin synthesis gene cluster from s. oneidensis under control of a medium Anderson promoter
BBa_K1913029BBa_K1913029 Version 1 (Component)Synthetic plac-FixK2 hybrid promoter +RBS with mRFP
BBa_K1913030BBa_K1913030 Version 1 (Component)Synthetic plac-FixK2 hybrid promoter+RBS with mRFP
BBa_K1913031BBa_K1913031 Version 1 (Component)Synthetic ptet-FixK2 hybrid promoter+RBS with mRFP
BBa_K2066124BBa_K2066124 Version 1 (Component)Synthetic Enhancer Project: UNS 52s NRII TetR
BBa_K2066123BBa_K2066123 Version 1 (Component)Synthetic Enhancer Project: UNS 55as NRII TetR
mbGHBBa_K2050413 Version 1 (Component)Synthetic bGh poly a tail with rabbit beta globin modification
BBa_K1363005BBa_K1363005 Version 1 (Component)R0082-HfiA the HfiA protein express passway which can be regulated by light
BBa_K152004BBa_K152004 Version 1 (Component)Promoterless Synthetic Operon of CrtE,B,I,Y
BBa_K337056BBa_K337056 Version 1 (Component)synthetic binding site of miR 122 (imperfect) KD: 64%
BBa_K337053BBa_K337053 Version 1 (Component)synthetic binding site of shRNA miRhaat (imperfect) KD:69 %%
BBa_K337052BBa_K337052 Version 1 (Component)synthetic binding site of shRNA miRhaat (perfect) KD:97%
BBa_K2123301BBa_K2123301 Version 1 (Component)Novel Synthetic Phytochelatin codon optimized for E. coli expression
BBa_K337057BBa_K337057 Version 1 (Component)synthetic binding site of miR 122 (imperfect) KD: 24%
BBa_K337054BBa_K337054 Version 1 (Component)synthetic binding site of shRNA miRhaat (imperfect) KD:28%
BBa_K152007BBa_K152007 Version 1 (Component)Synthetic operon of CrtEBIY and FrdBCD and GFP
BBa_K1124107BBa_K1124107 Version 1 (Component)pLac-hpaBC-plambda-sRNA(anti-tyrR)-plambda-sRNA (anti-csrA) (L-DOPA synthesis device)
BBa_K1172304BBa_K1172304 Version 1 (Component)Riboflavin synthesis gene cluster from s. oneidensis under control of T7 promoter and strong RBS
DiBBa_K1152004 Version 1 (Component)Expression cassette for NRPS that synthesizes a Pro-Leu-Dipeptide
BBa_K1170001BBa_K1170001 Version 1 (Component)Synthetic construct superfolder green fluorescent protein (sfgfp) gene, complete cds
BBa_K258012BBa_K258012 Version 1 (Component)AI2-dependent KGF synthesis with RFP reporter and AHL production for Quaroum Sensin Death Mechanism
BBa_J329030BBa_J329030 Version 1 (Component)QS System with BBa_J329998 Synthetic RBS + Const. RFP Expression
BBa_K2123204BBa_K2123204 Version 1 (Component)Bioaccumulator device: Strong promoter + OmpA fused to Synthetic Phytochelatin + B0015
BBa_K2066117BBa_K2066117 Version 1 (Component)Synthetic Enhancer: 2x TetO Binding Cassette + NRII on UNS
BBa_K152005BBa_K152005 Version 1 (Component)Promoterless Synthetic Operon of CrtE,B,I,Y and GFP
BBa_K2066118BBa_K2066118 Version 1 (Component)Synthetic Enhancer with 3X TetO cassette (52s) on UNS backbone
BBa_K2066113BBa_K2066113 Version 1 (Component)Synthetic Enhancer with 2X TetO cassette (55as) on UNS backbone
BBa_K1051262BBa_K1051262 Version 1 (Component)The measurement pathway of degradation tag K1051208.
BBa_K1051260BBa_K1051260 Version 1 (Component)The measurement pathway of degradation tag K1051206.
BBa_K1051261BBa_K1051261 Version 1 (Component)The measurement pathway of degradation tag K1051207.
BBa_K2066114BBa_K2066114 Version 1 (Component)Synthetic Enhancer: 3x TetO Binding Cassette (52s) + NRII on UNS
BBa_K2066112BBa_K2066112 Version 1 (Component)Synthetic Enhancer Project: Ntr promoter driven NRII2302 (mut) on UNS Standard
BBa_K1551000BBa_K1551000 Version 1 (Component)To generate delta-4 fatty acid Desaturase so as to synthesize the DHA.
SBOL Compliant SoftwareSBOLCompliantSoftware_collection Version 1 (Collection)A collection of software that supports the Synthetic Biology Open Language (SBOL) standard
BBa_K2066116BBa_K2066116 Version 1 (Component)Synthetic Enhancer Project: 3x TetO Binding Cassette (52s) + sfGFP on UNS
BBa_K2066115BBa_K2066115 Version 1 (Component)Synthetic Enhancer Project: 2x TetO Binding Cassette (55as) + sfGFP on UNS
BBa_K223021BBa_K223021 Version 1 (Component)SoxS + Part:BBa_K152005 (Promoterless Synthetic Operon of CrtE,B,I,Y and GFP)
BBa_K2066120BBa_K2066120 Version 1 (Component)Synthetic Enhancer Project: 3X TetO Binding Cassette(52S) + NRII + sfGFP on UNS
BBa_K2066119BBa_K2066119 Version 1 (Component)Synthetic Enhancer Project: 2X TetO Binding Cassette(52S) + NRII + sfGFP on UNS
BBa_K2066121BBa_K2066121 Version 1 (Component)Synthetic Enhancer Project: 2X TetO Binding Cassette(55aS) + NRII + TetR + sfGFP on UNS
BBa_K2066122BBa_K2066122 Version 1 (Component)Synthetic Enhancer Project: 3X TetO Binding Cassette(52S) + NRII + TetR + sfGFP on UNS
BBa_K2066549BBa_K2066549 Version 1 (Component)Synthetic Enhancer Project: RBS
iGEM Parts Registryigem_collection Version 1 (Collection)The iGEM Registry is a growing collection of genetic parts that can be mixed and matched to build synthetic biology devices and systems. As part of the synthetic biology community's efforts to make biology easier to engineer, it provides a source of genetic parts to iGEM teams and academic labs.
SEGASEGA_collection Version 1 (Collection)In the Standardized Genome Architecture (SEGA), genomic integration of DNA fragments is enabled by λ-Red recombineering and so-called landing pads that are a common concept in synthetic biology and typically contain features that i) enable insertion of additional genetic elements and ii) provide well-characterized functional parts such as promoters and genes, and iii) provides insulation against genome context-dependent effects. The SEGA landing pads allow for reusable homology regions and time-efficient construction of parallel genetic designs with a minimal number of reagents and handling steps. SEGA bricks, typically synthetic DNA or PCR fragments, are integrated on the genome simply by combining the two reagents (i.e. competent cells and DNA), followed by incubation steps, and successful recombinants are identified by visual inspection on agar plates. The design of the SEGA standard was heavily influenced by the Standard European Vector Architecture (SEVA). SEGA landing pads typically hosts two major genetic “control elements” that influence gene expression on the transcriptional (C1), and translational (C2) level. Furthermore, landing pads contain gadgets such as selection and counterselection markers.